Monitoring anticoagulation and inflammation in patients after heart and vascular surgery
Official title: Anticoagulation and Inflammation Monitoring in Patients After Heart and Vascular Interventions: Prospective Observational Study
Run by Medical University Innsbruck · NCT06222866 · Data updated 2026-11-12
This study is trying to find the best ways to monitor blood thinning treatments in patients after major heart and vascular surgeries to improve safety and outcomes.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 400 (estimated) |
| Sponsor | Medical University Innsbruck Academic / other |
| Locations | 1 site (Innsbruck, Tyrol) |
| Status | Recruiting |
| Started | June 25, 2024 |
| Main results expected | August 1, 2026 |
| Study ends | December 1, 2026 |
| Registry record updated | November 26, 2024 |
| Trial ID | NCT06222866 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include adults over 17 scheduled for elective cardiac or vascular surgery requiring anticoagulation.
✕Probably not a fit
Patients who are pregnant or participating in other interventional clinical trials may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to evaluate the most effective monitoring tools for unfractionated heparin (UFH) in patients undergoing major heart and vascular surgeries. It will compare various monitoring modalities, such as activated clotting time (ACT), activated partial thromboplastin time (aPTT), viscoelastic tests (ROTEM), and anti-Xa levels, to assess their association with adverse events like thrombosis and bleeding. Additionally, the study will explore the relationship between inflammation and delirium in these patients. By identifying the best monitoring practices, the study seeks to enhance patient safety and outcomes.
Why it matters
Potential benefit: If successful, this study could lead to improved anticoagulation management and reduced adverse events in patients undergoing heart and vascular interventions.
How similar studies have gone: While this study explores established monitoring techniques, the specific comparative approach to evaluate their effectiveness in this context is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age: \> 17 years * Informed written consent * Scheduled for cardiac intervention where the use of UFH is expected (elective surgery) * Scheduled for vascular intervention when the need for perioperative anticoagulation is expected (elective surgery) * Patients receiving ECMO support Exclusion Criteria: * Patients that are known to be pregnant * Known participation in other interventional clinical trial
Where it's running
-
Medical University Innsbruck
Innsbruck, Tyrol, Austria Recruiting
Study contacts
- Study coordinator: Sasa Rajsic, MD, PhD
- Email: sasa.rajsic@tirol-kliniken.at
- Phone: 004367763004447
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Can citicoline help prevent cognitive decline after delirium in older adults with hip fracture?
This study tests whether taking citicoline for 6 months after discharge helps prevent cognitive decline in adults 65 and older who had delirium during hospitalization for hip fracture.
-
Delirium and Light: Exploring Modifiable Risk Factors in Critically Ill Adults
This pilot observational study tests whether circadian-light factors influence delirium risk in adults recovering in critical care.
-
Appropriateness of Hemostatic Agent Use in Cardiovascular Surgery
This study tests how well surgeons’ choices about topical hemostatic agents match current guidelines in cardiac and vascular surgery at one Milan hospital.
-
VR-based cognitive games to help prevent delirium after big surgery
A VR-based cognitive stimulation game is being tested to see if it can help prevent delirium in adults 65 and older after major surgery.
-
Computer-assisted cognitive stimulation for delirium in older adults
This will try adding tablet-based cognitive exercises to sleep and mobility support to see if they reduce delirium in people aged 60 and older in subacute care.
-
Letting patients drink clear fluids until called to the operating room to shorten pre-surgery fasting
This project will try letting elective procedure patients drink clear liquids until they're called to the operating room to see if fasting times, comfort, and perioperative outcomes improve.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.